A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444873



Internal ID22111053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114658771..114658771hg38UCSC Ensembl
chr1:115201392..115201392hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759510
Samples
Known GenesDENND2C
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444873
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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